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Review
A Review on Antimicrobial Packaging for Extending the Shelf
Life of Food
Tobi Fadiji 1 , Mahdi Rashvand 2 , Michael O. Daramola 1 and Samuel A. Iwarere 1, *
Abstract: Food packaging systems are continually impacted by the growing demand for minimally
processed foods, changing eating habits, and food safety risks. Minimally processed foods are
prone to the growth of harmful microbes, compromising quality and safety. As a result, the need for
improved food shelf life and protection against foodborne diseases alongside consumer preference for
minimally processed foods with no or lesser synthetic additives foster the development of innovative
technologies such as antimicrobial packaging. It is a form of active packaging that can release
antimicrobial substances to suppress the activities of specific microorganisms, thereby improving food
quality and safety during long-term storage. However, antimicrobial packaging continues to be a very
challenging technology. This study highlights antimicrobial packaging concepts, providing different
antimicrobial substances used in food packaging. We review various types of antimicrobial systems.
Emphasis is given to the effectiveness of antimicrobial packaging in various food applications,
including fresh and minimally processed fruit and vegetables and meat and dairy products. For
the development of antimicrobial packaging, several approaches have been used, including the
use of antimicrobial sachets inside packaging, packaging films, and coatings incorporating active
antimicrobial agents. Due to their antimicrobial activity and capacity to extend food shelf life,
regulate or inhibit the growth of microorganisms and ultimately reduce the potential risk of health
hazards, natural antimicrobial agents are gaining significant importance and attention in developing
antimicrobial packaging systems. Selecting the best antimicrobial packaging system for a particular
product depends on its nature, desired shelf life, storage requirements, and legal considerations. The
Citation: Fadiji, T.; Rashvand, M.; current review is expected to contribute to research on the potential of antimicrobial packaging to
Daramola, M.O.; Iwarere, S.A. A
extend the shelf life of food and also serves as a good reference for food innovation information.
Review on Antimicrobial Packaging
for Extending the Shelf Life of Food.
Keywords: food packaging; antimicrobial agent; active packaging; shelf life; fruit and vegetables;
Processes 2023, 11, 590. https://
meat products
doi.org/10.3390/pr11020590
Figure 1. Illustration of the active scavenging and releasing systems used in food packaging.
Figure 1. Illustration of the active scavenging and releasing systems used in food packaging.
Over the
Over the years,
years, consumers’
consumers’ surge
surge of
of interest
interest in
in minimally
minimally processed
processed and
and additive-
additive-
free foods has resulted in the ongoing development of an intriguing innovation
free foods has resulted in the ongoing development of an intriguing innovation in in active
active
packaging known as antimicrobial packaging [10,20]. Antimicrobial packaging
packaging known as antimicrobial packaging [10,20]. Antimicrobial packaging systems systems
are based on packaging materials with incorporated antimicrobial agents in the packaging
matrix and/or antimicrobial polymers [20]. When a packaging system (or material) obtains
antimicrobial activity, it inhibits or prevents microbial development by extending the lag
time and reducing the growth rate or decreasing microbe live counts. Hence, antimicrobial
packaging helps inhibit spoilage and reduce pathogenic microorganisms by incorporating
packaging with antimicrobials, consequently extending food shelf life by prolonging the lag
Processes 2023, 11, 590 3 of 30
period of microorganisms, thereby diminishing their growth and number [20,29]. Antimi-
crobial packaging is intended to act against microorganisms and enhance the functions of
conventional food packaging, which are (1) shelf life extension, (2) maintenance of quality,
and (3) safety assurance [15,22,29].
There are several excellent recent reviews on food packaging systems, particularly
with active characteristics, including active packaging in the food industry/foods [23,25,30],
active packaging coatings [28,31], active edible films and packaging [31–33], natural antiox-
idants in active food packaging [34], innovative active, intelligent and smart packaging
technologies [35], active packaging applications to muscle foods [36], active packaging films
in the meat industry [37], active packaging in bakery products [38], and pectin-based active
packaging [39], to name a few examples. Given the promising reports and interventions
in antimicrobial packaging research to extend food shelf life and ensure food safety by
inhibiting microbial growth in packaged foods and packaging materials, this research area
has emerged as an independent focus area with positive consumer response. Therefore,
this current review provides a focused and precise concept of antimicrobial packaging for
extending the shelf life of food, emphasizing selected representative publications within
the last decade.
Various antimicrobial agents may be incorporated into packaging systems. They in-
clude organic acids, mineral acids, inorganics, phenolic compounds, and isothiocyanates [22].
These antimicrobial agents can be categorized into natural or chemical (synthetic) agents.
Their application often depends on the packaging material. For instance, studies proposed
that potassium sorbate and nisin antimicrobial compounds added to a chitosan matrix
to create an active packaging film reduced the resistance and increased the flexibility of
the active film [52]. Similarly, Sung et al. [53] added Allium sativum essence oil (AEO)
into plastic films to test for antimicrobial activities against beef-related bacteria, namely
Listeria monocytogenes, Escherichia coli, and Brochothrix thermosphacta. The film’s mechan-
ical properties were slightly affected by the AEO, and a significant increase in the film
crystallinity with a small amount of incorporated AEO was reported [53].
Despite the approval of chemical antimicrobial agents (sodium benzoates and propi-
onates, potassium sorbates, sorbic acid, sulfites, chlorides, nitrites, triclosan, nisin, tartaric
acid, etc.) by regulatory agencies, many of these agents continue to pose nutritional or
health threats for the end-users [54–57]. As a result, natural antimicrobial agents are gaining
much importance and attention due to their antimicrobial activity potential to extend food
shelf life and control or prevent the growth of microorganisms [54,58,59]. Additionally,
consumer awareness of the potential adverse effect of synthetic or chemical preservatives
versus the advantages of natural additives/alternatives has increased the interest in de-
veloping and using natural products for food preservation and microorganism control
or prevention. These are commonly referred to as natural antimicrobial agents. Natural
additives come from organic matter and can be obtained from plants, animals, fungi, and
algae; hence, they reduce exposure to potential health hazards [55].
The extensive application of natural antimicrobial agents, primarily as preservatives
in fruit and vegetables, has been reported to ensure safety, protect the quality, and extend
shelf life [55]. Natural antimicrobials are secondary metabolites possessing antimicro-
bial activity [54,55,60]. They have antibacterial and antioxidant properties and are con-
sidered preferable alternatives to synthetic antimicrobials because they can be derived
from various sources, including plants, animals, and microorganisms which are the most
common [58,61–63]. According to several studies, most important natural antimicrobial
compounds are essential oils obtained from plants (e.g., basil, thyme, oregano, cinnamon,
clove, sage, vanillin, and rosemary); enzymes obtained from animal sources (e.g., lysozyme,
lactoferrin), bacteriocins from microbial sources (nisin, natamycin, lactocin, pediocin) and
organic acids (e.g., sorbic, propionic, citric acid) and naturally occurring polymers (chi-
tosan) [54,64,65].
Plants are considered the most important and rich natural source of antimicrobial
substances [54]. These plant compounds have antimicrobial, antioxidant, flavor, and color-
enhancing properties. These plant agent qualities lengthen the product’s shelf life and
improve its organoleptic acceptability. These compounds serve an important function
in inhibiting the growth of foodborne pathogens and, as a result, lowering the risk of
disease [54,62]. Therefore, they build consumer confidence regarding the consumption of
food products. Commercially based plant-origin antimicrobials are commonly produced by
SD (steam distillation) and HD (hydro-distillation) methods as well as alternative methods
such as SFE (supercritical fluid extraction) from aromatic and volatile oily liquids from
flowers, buds, seeds, leaves, twigs, bark, herbs, wood, fruits, and roots of plants [54].
The antimicrobial substances used to activate packaging materials can be included in
the groups of metals, chemicals, plant extracts, enzymes, and bacteriocins. The activities
of each address a restricted group of microorganisms, but their actions can be combined
with those of other hurdles to enlarge the spectrum of microbial targets. To inhibit the
growth of undesired microbes in food, natural antimicrobials can be directly added to the
product composition, coated on its surface, or incorporated into the packaging material.
Introducing active agents into food results in an immediate but short decrease in microbial
pathogens, whereas antimicrobial films can sustain their activity for an extended time [54].
Processes 2023, 11, 590 5 of 30
Antimicrobial packaging has attracted the attention of many researchers due to the
variety of materials used, its advantages and disadvantages, and the ability to improve
the shelf life of food and agricultural products. Most importantly, they help reduce,
inhibit, or retard spoilage microorganisms’ growth in food products, thus preventing food
spoilage and decay. One of the current challenges is the impact of antimicrobial agents
on packaging properties. For instance, the polymer is common for fabricating packaging
layouts [46], and studies have shown that antimicrobial agents alter the barrier properties
of polymer films [66,67]. Incorporating antimicrobial agents into polymer films enhances
the hydrophobic ratio, increasing the transfer coefficient while decreasing the water vapor
permeability (WVP) [68]. Furthermore, some antimicrobial agents, such as lactoperoxidase,
lysozyme, and lactoferrin, reduce the permeability properties of polymers [69]. Hence,
the use of nano-clay in combination with a polymeric material has been recommended by
different studies to improve the mechanical, thermal, and permeability properties [70–72].
In some cases, combining antimicrobial agents with polymers might have drawbacks
that limit large-scale production and increase production costs [73]. Although integrating
antimicrobial agents and polymers by extrusion is straightforward, some of the antimi-
crobial agents evaporate due to the high temperature caused by the extrusion process.
Furthermore, due to antimicrobial agent dispersion, the extrusion process results in antimi-
crobial agent loss [74]. As a result, researchers apply antimicrobial agents to the adhesive
layer that links the laminate’s various layers [75,76]. It has also been proposed to use
antimicrobial agent bags in inclusion complexes (ICs) [77,78]. Some researchers, however,
do not endorse this strategy due to customer reluctance to purchase this type of packaging.
Hence, various antimicrobial agents, including ICs, are inserted at the package’s bottom or
head (in the form of two or more layers) [79–81]. Table 1 shows the application of various
antimicrobial agents in previous research.
Table 1. Overview of the use of several antimicrobial agents in various products.
Figure 2 illustrates an antimicrobial system and the relative behavior of active substances.
Figure 2. Antimicrobial
Figure 2. Antimicrobial packagingpackaging system(adapted
system (adapted from Jideani
from and Vogtand
Jideani (2016)Vogt
[22] and Han [22] and Han
(2016)
(2003) [91]).
(2003) [91]).
In Figures 2A,B, antimicrobial agents are released through diffusion between the
packaging material and the food and partitioning at the interface. The inclusion of the
antimicrobial agent into the packaging material is chemically bonded via immobilization
(Figure 2A). In Figure 2A, the antimicrobial agent is incorporated into the packaging ma-
terial. To regulate the release rate, particularly in the two-layer system (Figure 2B), the
antimicrobial agent (outer layer) is coated on the packaging material (inner layer), or the
antimicrobial matrix layer (outer layer) is laminated with the control layer (inner layer).
Figure 2C depicts a headspace system. Here, the volatile antimicrobial agent initially in-
Processes 2023, 11, 590 7 of 30
In Figure 2A,B, antimicrobial agents are released through diffusion between the pack-
aging material and the food and partitioning at the interface. The inclusion of the antimicro-
bial agent into the packaging material is chemically bonded via immobilization (Figure 2A).
In Figure 2A, the antimicrobial agent is incorporated into the packaging material. To
regulate the release rate, particularly in the two-layer system (Figure 2B), the antimicrobial
agent (outer layer) is coated on the packaging material (inner layer), or the antimicrobial
matrix layer (outer layer) is laminated with the control layer (inner layer). Figure 2C
depicts a headspace system. Here, the volatile antimicrobial agent initially integrated
into the matrix layer is released into the headspace. Equilibrated sorption/isotherm is
used to partition the headspace antimicrobial agent from the food product. A headspace
system with a control layer is shown in Figure 2D. The control layer precisely regulates
the permeability of the volatile antimicrobial agent and maintains a specific headspace
concentration [91,92]. Figure 2C,D show that the antimicrobial agent’s volatility permits it
to reach the gaseous-phase particle’s headspace to contact the food product.
The antimicrobial properties of ethanol are widely known. Ethanol generators reduce
the rate of staling and oxidative changes in foods such as cheeses, bread, and bakery prod-
ucts as well as the incidence of microbial deterioration [16]. Encapsulated ethanol sachets
emit their vapor into the package headspace, maintaining the preservation effect [103,104].
However, one disadvantage is the typical off-flavor of ethanol. Ethanol generators ef-
fectively control about ten species of mold, including Aspergillus and Penicillium species,
different species of bacteria, including Salmonella, Staphylococcus, and E. coli, as well as
species of spoilage yeast [105].
Chlorine dioxide (ClO2 ) is a powerful oxidizing and sanitizing agent used in gaseous or
aqueous forms to wash fresh produce to keep them safe from bacterial contamination [106,107].
The effectiveness of chlorine dioxide generators in controlling pathogenic and spoilage mi-
croorganisms, thereby increasing food product shelf life, was reported by [108]. Ray et al.
(2013) developed a chlorine dioxide (ClO2 )-releasing packaging for fresh produce decontami-
nation. The authors found that the released ClO2 reduced Salmonella spp. and E. coli O157:H7
inoculated on the tomatoes to undetectable levels [109].
While sachets, pouches, and pads have several benefits, they have a few drawbacks.
Because sachets and pads are often placed in each package manually, packaging time
is increased, thereby limiting productivity [95,110]. Another drawback is the inability
to use them in liquid foods. Liquids touching the sachet material may cause leakage
of its contents. Another disadvantage is consumer acceptability. Loose sachets may be
mistaken for food, posing a concern due to the risk of disintegration, contamination, and
unintentional consumption [95].
polymeric matrices to provide antimicrobial activity and improve packaging qualities [125].
Table 2 highlights examples of chitosan films enhanced with polymers and nanomaterials.
Table 2. Some examples of studies with chitosan film enhanced with polymers and nanomaterials.
Packaging Material
(Chitosan + Polymer, Target Microorganism Antimicrobial Functionality Reference
Chitosan + Nanomaterial)
Chitosan + Gallic acid Two Gram-negative bacteria: E. coli and Gallic acid significantly increased the [126]
Salmonella typhimurium, and two antimicrobial activities of chitosan films
Gram-positive bacteria: Bacillus subtilis
and Listeria innocua
Chitosan + Maqui berry L. innocua, Serratia marcescens, Pure chitosan film effective against only [127]
(MB) extracts Aeromonas hydrophila, S. putrefaciens and P. fluorescens
Achromobacter denitrificans, Chitosan with MB films were effective
Alcaligenes faecalis, Pseudomonas against all the bacteria except L. innocua
fluorescens, Citrobacter freundii and
Shewanella putrefaciens
Chitosan film + Propolis Gram-positive bacteria (S. aureus) and Chitosan alone did not show any [128]
extract (PE) Gram-negative bacteria (E. coli, inhibition against tested bacteria
Pseudomonas aeruginosa, Antimicrobial activity was evident for
and Salmonella Enteritidis) chitosan + PE
Chitosan + Rosemary Listeria monocytogenes, Pseudomonas Notable inhibitory activity [129]
essential oil (REO) putida, Streptococcus agalactiae, E. coli, on microorganisms
and Lactococcus lactis
Chitosan + Glycerol E. coli, S. aureus and A. niger High content of chitosan film had [130]
antimicrobial properties compared with
a low chitosan content film
Chitosan film with increasing glycerol
had no bacteriostatic effect
Chitosan + Peptide E. coli and B. subtilis All developed films exhibited [131]
antibacterial activity
No significant improvement in
antibacterial activity with the addition
of soy or corn peptides
Chitosan + Squid Aspergillus parasiticus Fungistatic activity of the chitosan films [132]
gelatin hydrolysates (SGH) was not significantly improved with the
addition of 10% SGH
Fungistatic index increased by 34% by
adding 20% SGH
Chitosan + Olive leaf E. coli, L. monocytogenes, and Chitosan + OLE films have significant [133]
extract (OLE) Campylobacter jejuni subsp. jejuni antimicrobial activity against
L. monocytogenes and C. jejuni but are
not evident for E. Coli.
Chitosan + AgNPs or Zinc S. aureus, E. coli, Salmonella typhamrium, Developed chitosan nanocomposite [134]
oxide nanoparticles (ZnONPs) B. cereus, and Listeria monocyte. films showed high
antimicrobial activity
Chitosan + ZnONPs Gram-positive bacterium Twofold and 1.5-fold increment in the [135]
Bacillus subtilis (B. subtilis) and antimicrobial activity was observed for
Gram-negative bacterium (E. coli) B. subtilis and E. coli, respectively, with
increased ZnONPs concentration in the
films from 0(w/w) to 2%(w/w)
Chitosan + AgNPs Gram-positive bacteria: S. aureus and Developed film significantly inhibited [136]
pathogenic yeast: Candida albicans the growth of S. aureus and showed
(C. albicans) marked antifungal activity against
C. albican
Chitosan + ZnONPs + Gram-positive B. subtilis and Resultant film was efficient against the [137]
Gallic acid Gram-negative E. coli microorganisms and has a great
potential application for improving the
shelf life of food products
Processes 2023, 11, 590 10 of 30
Table 2. Cont.
Packaging Material
(Chitosan + Polymer, Target Microorganism Antimicrobial Functionality Reference
Chitosan + Nanomaterial)
Chitosan/pullulan (CS/PL) Pseudomonas aeruginosa (P. aeruginosa), Developed film enhanced antioxidant [138]
nanocomposite films + clove S. aureus, and E. coli activity and showed strong
essential oil (CEO) loaded antibacterial activity against the
Chitosan-ZnO target microorganisms
hybrid nanoparticles
Chitosan/Zein films + P. aeruginosa, B. subtilis, E. coli Bacterial growth of S. aureus, B. subtilis [139]
Mosla chinensis EOs and S. aureus and E. coli was inhibited in both
nanoemulsions (NEs) and NPs EO-loaded NP and NE films.
Chitosan + polyvinyl alcohol E. coli, S. aureus, A. niger and C. albicans Nanocomposites films had good [140]
(PVA) + Fe2 O3 /TiO2 antibacterial activity
(FeTiO2 ) NPs
Chitosan + Guar gum + PVA + E. coli and S. aureus PVA and guar gum did not show any [141]
Moringa extract (ME) antibacterial activity
Incorporating ME enhanced the
antibacterial activity against S. aureus
and E. coli bacteria
Chitosan + turmeric essential Bacillus cereus TEO exhibited antioxidant and [142]
oil (TEO) + magnetic-silica antibacterial activities against
nanocomposites Bacillus cereus
Chitosan film incorporated with the
bionanocomposite had a stronger
antibacterial effect against B. cereus than
the chitosan film containing only TEO
Sun et al. [126] prepared chitosan film with different gallic acid concentrations. The
authors evaluated the developed films’ antimicrobial, mechanical, physical, and structural
properties. Antimicrobial activity was assessed against two Gram-negative bacteria, E. coli
and Salmonella typhimurium, as well as two Gram-positive bacteria, B. subtilis, and L. innocua.
Chitosan films infused with gallic acid considerably increased their antimicrobial properties,
and the films reduced microbial growth by 2.5-log reduction. In another recent investigation,
Li et al. [131] developed chitosan/peptide films by incorporating peptides (0.4%, w/v) from
soy, corn, and caseins into chitosan films. Peptides are protein fragments that exist as host
defense molecules in the innate immune systems of invertebrates and vertebrates with
unique functional activities (e.g., antimicrobial, antioxidant, antithrombotic) [143]. The
antibacterial activity of films was tested against E. coli and B. subtilis. Due to the presence
of chitosan, all the films demonstrated antimicrobial activity. The inclusion of soy or corn
peptides did not significantly increase the antibacterial activity of the films. However,
adding casein peptides increased the film’s antibacterial activity and inhibited the growth
of E. coli and B. subtilis.
Qin et al. [144] developed active packaging films by integrating AgNPs and anthocyanin-
rich purple corn extract (PCE) into chitosan. The chitosan/AgNPs/PCE film had the
best barrier, mechanical, antioxidant, and antimicrobial properties [144]. Enhanced an-
timicrobial activity was shown against four foodborne pathogenic bacteria strains (E coli,
S. aureus, Salmonella, and L. monocytogenes). Notably, the chitosan/AgNPs/PCE film’s
antimicrobial properties were the strongest, while the chitosan/PCE film had the lowest
antimicrobial properties. The enhanced activity could be related to AgNPs’ interaction
with membrane proteins, enzymes, and nucleic acids, leading to cell lysis and death [145],
and the presence of abundant anthocyanins in PCE [127,146]. Mohamed and Madian [136]
successfully developed chitosan films doped with silver nanoparticles. The authors showed
that incorporating silver nanoparticles into chitosan film significantly increased its mechan-
ical characteristics and antimicrobial activity. Compared with pure chitosan film, silver
nanoparticles doped with chitosan films showed significant antibacterial activity against
Processes 2023, 11, 590 11 of 30
S. aureus [136]. Yadav et al. [137] developed an active packaging film made of chitosan and
ZnONPs loaded with gallic acid (Ch-ZnO@gal) using the casting method. The antibacte-
rial activity of the films was evaluated against both bacterial strains, i.e., Gram-positive
B. subtilis and Gram-negative E. coli. The developed film possessed significant antibacterial
potential compared to pure chitosan film. The findings were related to the impact of reactive
oxygen species released by ZnONPs loaded with gallic acid and Zn2+ ions. They attack the
negatively charged cell wall, causing leakage and, eventually, bacterial death [147–149].
coated PLA films [166], bacteriocins-coated polyethylene terephthalate (PET) films [167],
plantaricin BM-1 and chitosan-coated polyethylene terephthalate/polyvinylidene chlo-
ride/retort casting polypropylene (PPR) plastic [168], etc.
Table 3. Cont.
sine as the immobilized antimicrobial, and dicumyl peroxide as the free radical initiator and
cross-linker. After 1 h of incubation at 37 ◦ C, the antimicrobial active packaging material
reduced P. aeruginosa by 1-log [185].
6.1. Antimicrobial Packaging for Fresh and Minimally Processed Fruits and Vegetables
Fresh and minimally processed fruits and vegetables are perishable and easily com-
promised by postharvest physiological changes and microbial contamination throughout
postharvest transportation, processing, storage, and retail display [116,186]. Minimally pro-
cessed foods and vegetables, for instance, are extensively researched due to the difficulty in
retaining their fresh-like quality over lengthy periods, and the goal of minimally processed
products is to provide convenience and excellent quality [54]. Incorporating antimicrobial
agents into the packaging of fruits and vegetables could be a strategy for controlling the
effects of microorganisms, extending shelf life, and providing higher quality products. As
reported by Giannakourou and Tsironi [42] and Jung and Zhao [186], there are three forms
of antimicrobial packaging that have been documented for use on fresh and minimally
processed fruits and vegetables, namely:
1. Antimicrobial sachets: sachets containing volatile antimicrobial agents enclosed in
the packaging;
2. Antimicrobial films: the inclusion of volatile or nonvolatile antimicrobial chemicals
into packaging film composition;
3. Antimicrobial edible coatings: directly applying antimicrobial edible coatings or films
to the food surface.
Antimicrobial systems employ synthetic and natural active agents to inhibit microbial
development, as previously discussed. Essential oils (EO) and plant extracts, organic acids
and their salts, and chitosan are a few examples. Metals and metal oxides such as silver
(Ag) and zinc oxide (ZnO) have also demonstrated significant promise as antimicrobial
packaging agents to create more cost-effective and safe food packaging solutions for fruits
and vegetables [187]. Table 4 presents some examples of developed antimicrobial systems
to reduce microbial growth in fruit and vegetables.
Processes 2023, 11, 590 15 of 30
Table 4. Summary of examples of antimicrobial packaging systems utilized to reduce microbial growth in fruit and vegetables.
Table 4. Cont.
agents in films). However, studies have shown that they are unsuitable for meat products
and that recycling is challenging [47,208]. As a result, biodegradable polyurethane was
proposed as a meat packaging material. Natural biopolymers (chitosan), organic acids or
their related acid anhydrides, alcohols, bacteriocins (nisin and pediocin), chelators, and
enzymes (lysozyme), among others, are some of the types of antimicrobial agents suggested
and investigated for meat packaging problems [24,181]. Although the inclusion of lactic
acid bacteria (LAB) into biopolymer films is an intriguing novel approach [181], these
bacteria are resistant to CO2 , which is widely used in vacuum or modified atmosphere
packaging (MAP) [209]. Additionally, while exposing meat products to antimicrobial
agents such as essential oils have some influence on microbial development, the adverse
organoleptic effects of the intense odor caused by application to meat limit their use to a
certain extent [206].
Recent research provides new insights into the efficiency of antimicrobial compounds
and silver-containing packaging in preventing beef deterioration [210,211]. Some re-
searchers, however, have pointed out the drawbacks of employing silver to restrict an-
tibacterial packaging. As a result, the use of nanoparticle coating during the packaging
process of meat products, including antibacterial compounds as well as silver, was recom-
mended [85,212,213]. For instance, Soysal et al. [86] investigated the impact of antimicrobial
agents (nisin, chitosan, potassium sorbate (PS), or silver substituted zeolite (AgZeo)) incor-
porated into low-density polyethylene (LDPE) on the physicochemical and microbiological
quality of chicken drumsticks. The use of active bags resulted in a lower level of total
aerobic mesophilic bacteria (APC), total coliform, mold, and yeast count in chicken drum-
sticks. The chitosan-containing film was the most successful in extending the shelf life and
improving the quality of the drumsticks. At 5 ◦ C for 6 days, the active bags reduced APC
and total coliform in the order chitosan > nisin > AgZeo > PS, while mold and yeasts were
reduced in the sequence chitosan > PS > nisin > AgZeo > PS.
Overall, the meat products’ packaging methods depend on the reaction of the used
materials and the antimicrobial agents. Table 5 summarizes the use of antimicrobial agents
in packaging various meat products and the objective of the previous investigations.
Table 5. Antimicrobial packaging and its application for meat products.
Table 6. Cont.
Union), and others. They establish the legal foundation for their correct use, safety, and mar-
keting [7,27]. The active (antimicrobial) compound and the inert carrier are the two primary
components of an active antimicrobial system. Active agents being purposely released
from the packaging system into the food would fall under food additives. Hence, they
must meet specific scientific and technological standards, while the carrier must fulfil the
safety criteria for food contact materials [240]. Often, standards for food contact materials
are stringent to avoid the migration of undesired components into the food. Understanding
appropriate regulatory choices, as well as environmental sustainability problems, would
aid commercialization efforts. Finally, consumer acceptability and purchase intent boost
the adoption of innovative packaging technologies, notably antimicrobial active packaging.
8. Conclusions
The technology of antimicrobial packaging is rapidly evolving. This method employs
antimicrobial agents or substances in a polymer matrix to reduce the growth of spoilage
food pathogens by targeting specific microorganisms to extend food shelf life. A thorough
understanding of antimicrobial packaging enables researchers and food industries to
develop appropriate methods for reducing microbial risks and improving food quality.
This review provided a comprehensive basic concept of antimicrobial packaging technology
and a summary of recent studies on antimicrobial packaging to extend the shelf life of
food products, emphasizing fresh and minimally processed fruits and vegetables, meat,
and dairy products. Although potent in reducing the growth of microbes in food, the
effectiveness and synergistic effects of antimicrobial packaging can be improved when
combined with other preservation hurdles, which may be dependent on the spoilage
properties, required shelf life, and consumer preferences. However, some issues exist,
including recycling management, reasonable prices for producers and consumers, and the
complexity of the production process are challenges for scientists and researchers. The
shelf life and safety of fresh fruits, vegetables, dairy, and meat products can be enhanced
by adjusting the level of active agents in the packages. Additionally, an inspection of the
diffusion rate of the antimicrobial agents from the film and their subsequent effectiveness
on food products from the chemical view is still debatable. For this reason, establishing
a multidisciplinary approach is imperative based on the scientific work of researchers
and scholars. Furthermore, increasing the effectiveness and efficiency of antimicrobial
packaging necessitates the identification of more natural antimicrobial compounds that are
effective in improving their stability in packaging systems and ensuring the safety of their
commercial applications. Similarly, for any application, selecting the best antimicrobial
packaging systems for a given product is essential. The selection can be determined by the
nature of the produce, storage conditions, required shelf life, and regulatory requirements.
Author Contributions: Conceptualization, T.F. and M.R.; methodology, T.F. and M.R.; writing—original
draft preparation, T.F. and M.R.; writing—review and editing, T.F., M.R., S.A.I. and M.O.D.; funding ac-
quisition, S.A.I. and M.O.D. All authors have read and agreed to the published version of the manuscript.
Funding: This work is funded by the Department of Chemical Engineering of the University of
Pretoria and Faculty of Engineering, the Built Environment and Information Technology, Pretoria,
South Africa. The corresponding author – Samuel A. Iwarere is funded by the Government of the
United Kingdom through The Royal Society as a FLAIR Fellow [FLR\R1\201683].
Data Availability Statement: Not applicable.
Conflicts of Interest: The authors declare no conflict of interest.
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